Novel piperidine compounds

ABSTRACT

Novel piperidine compounds of the general formula (I) ##STR1## in which m is an integer from 1 to 4, R 1  and R 2  are as defined in claim 1 and at least one 2,2,6,6-tetramethylpiperidinyl group, being present in R 1  or R 2  are useful as light stabilizers, heat stabilizers and oxidation stabilizers for organic material, especially for synthetic polymers.

The present invention relates to novel piperidine compounds and theiruse as light stabilisers, heat stabilisers and oxidation stabilisers fororganic material, especially for synthetic polymers.

In order to delay the negative effect of ultraviolet radiation onpolymers, it has been proposed to use various stabilisers which protectagainst light; in particular, U.S. Pat. No. 4,525,503 describespiperidine esters of carbamic acids.

The present invention is concerned with novel oxamates of the generalformula (I) ##STR2## in which m is an integer from 1 to 4 and, if m=1,R₁ is a group ##STR3## in which R₃ and R₄ are identical or different andare hydrogen, C₁ -C₁₈ -alkyl, C₂ -C₆ -alkyl substituted by a C₁ -C₁₈-alkoxy or by a C₂ -C₁₈ -dialkylamino, C₅ -C₁₈ -cycloalkyl, C₃ -C₁₈-alkenyl, C₆ -C₁₈ -aryl unsubstituted or substituted by C₁ -C₁₂ -alkoxy,by C₁ -C₁₂ -alkyl and/or by --OH, C₇ -C₁₈ -aralkyl unsubstituted orsubstituted by C₁ -C₁₂ -alkyl and/or by --OH or are a group of theformula (II) ##STR4## where R₅ is hydrogen, O., cyanomethyl, C₁ -C₁₂-alkyl, C₃ -C₁₂ -alkenyl, C₃ -C₁₂ -alkynyl, C₇ -C₁₂ -aralkylunsubstituted or substituted by C₁ -C₁₂ -alkyl, or is C₁ -C₁₂ -acyl, orR₁ is a 5-membered to 13-membered heterocyclic group containing at leastone nitrogen atom being linked to the

    --COCOOR.sub.2 radical,

or if m=2, R₁ is a group ##STR5## in which R₆, R₈, R₉ and R₁₀ areidentical or different and are hydrogen, C₁ -C₁₈ -alkyl, C₅ -C₁₈-cycloalkyl unsubstituted or substituted by C₁ -C₁₂ -alkyl, C₃ -C₁₈-alkenyl, C₆ -C₁₈ -aryl unsubstituted or substituted by C₁ -C₁₂ -alkoxy,by C₁ -C₁₂ -alkyl and/or by --OH, C₇ -C₁₈ -aralkyl unsubstituted orsubstituted by C₁ -C₁₂ -alkyl and/or by --OH, or are a group of theformula (II) and R₇ ist C₂ -C₁₈ -alkylene, C₆ -C₁₈ -cycloalkylene, C₆-C₁₈ -arylene, C₇ -C₁₈ -aralkylene or a group --R₁₁ --X--(R₁₂ --X)_(n)--R₁₁ --, where R₁₁ and R₁₂ are identical or different and are C₂ -C₆-alkylene and X is --O-- or ##STR6## R₁₃ being hydrogen, C₁ -C₁₂ -alkyl,C₅ -C₁₂ -cycloalkyl unsubstituted or substituted by C₁ -C₁₂ -alkyl, or agroup of the formula (II) and n is zero, 1 or 2, or R₁ is a 5-memberedto 7-membered divalent heterocyclic group containing 2 nitrogen atomsbeing linked to the

    --COCOOR.sub.2 radicals,

or if m=3, R₁ is a group ##STR7## in which R₁₄ and R₁₇ are identical ordifferent and are hydrogen, C₁ -C₁₈ -alkyl, C₅ -C₁₂ -cycloalkylunsubstituted or substituted by C₁ -C₁₂ -alkyl, C₇ -C₁₈ -aralkylunsubstituted or substituted by C₁ -C₁₂ -alkyl and/or by --OH, or are agroup of the formula (II) and R₁₅ and R₁₆ are identical or different andare C₂ -C₆ -alkylene, or R₁ is a hexahydro-1,3,5-triazine-1,3,5-triylgroup, or if m=4, R₁ is a group ##STR8## in which R₁₈ and R₂₂ areidentical or different and are as defined for R₁₄ and R₁₇, while R₁₉,R₂₀ and R₂₁ are identical or different and are C₂ -C₆ -alkylene, or R₁is a group ##STR9## in which R₂₃, R₂₄, R₂₅ and R₂₆ are identical ordifferent and are C₂ -C₆ -alkylene, R₂ is C₁ -C₁₈ -alkyl, C₅ -C₁₈-cycloalkyl unsubstituted or substituted by C₁ -C₁₂ -alkyl, C₃ -C₁₈-alkenyl, C₆ -C₁₈ -aryl unsubstituted or substituted by C₁ -C₁₂ -alkoxy,by C₁ -C₁₂ -alkyl and/or by --OH, C₇ -C₁₈ -aralkyl unsubstituted orsubstituted by C₁ -C₁₂ -alkyl and/or by --OH, or is a group of theformula (II) or, if m is 1 and R₁ is a group ##STR10## R₂ additionallyis a group of the formula (III) ##STR11## wherein R₃ and R₅ are asdefined above and R₂₇ is C₂ -C₁₂ -alkylene, C₆ -C₁₈ -cycloalkylene orone of the following groups ##STR12## in which R₂₈ is hydrogen or C₁ -C₄-alkyl, R₂₉ is hydrogen, C₁ -C₄ -alkyl or a group ##STR13## R₃ and R₅are as defined above and p is an integer from 1 to 4, at least one groupof the formula (II) being present in R₁ R₂.

Illustrative examples of the meaning of the various groups are asfollows:

for R₃ R₄ : hydrogen, methyl, ethyl, propyl, isopropyl, butyl, 2-butyl,isobutyl, t-butyl, hexyl, octyl, 2-ethylhexyl, 1,1,3,3-tetramethylbutyl,decyl, dodecyl, tetradecyl, hexadecyl, octadecyl, 2-methoxyethyl,2-ethoxyethyl, 3-methoxypropyl, 3-ethoxypropyl, 3-butoxypropyl,3-octyloxypropyl, 3-dodecyloxypropyl, 3-dimethylaminopropyl,3-diethylaminopropyl, 4-diethylaminobutyl, cyclohexyl, methylcyclohexyl,trimethylcyclohexyl, cyclooctyl, cyclododecyl, allyl, 2-methallyl,2-butenyl, 2-hexenyl, 10-undecenyl, oleyl, phenyl, methylphenyl,dimethylphenyl, trimethylphenyl, t-butylphenyl, methoxyphenyl,ethoxyphenyl, 3,5-di-t-butyl-4-hydroxyphenyl, benzyl, methylbenzyl,hydroxybenzyl, 3,5-di-t-butyl-4-hydroxybenzyl,2,2,6,6-tetramethylpiperidin-4-yl, 1,2,2,6,6,-pentamethylpiperidin-4-yl,1-allyl-2,2,6,6-tetramethylpiperidin-4-yl,1-benzyl-2,2,6,6-tetramethyl-piperidin-4-yl and1-acetyl-2,2,6,6-tetramethylpiperidin-4-yl;

for R₅ : hydrogen, O., cyanomethyl, methyl, ethyl, propyl, butyl, hexyl,octyl, decyl, dodecyl, allyl, 2-methallyl, 2-butenyl, 2-hexenyl,10-undecenyl, propargyl, benzyl, methylbenzyl, t-butylbenzyl,hydroxybenzyl, formyl, acetyl, propionyl, butyryl, caproyl, capryloyl,caprinoyl, lauroyl, benzoyl, acryloyl, methacryloyl and crotonyl;

for R₆, R₈, R₉ and R₁₀ : hydrogen, methyl, ethyl, propyl, isopropyl,butyl, 2-butyl, isobutyl, t-butyl, hexyl, octyl, 2-octyl, 2-ethylhexyl,1,1,3,3-tetramethylbutyl, decyl, dodecyl, tetradecyl, hexadecyl,octadecyl, cyclopentyl, cyclohexyl, methylcyclohexyl,trimethylcyclohexyl, cyclooctyl, cyclododecyl, allyl, 2-methallyl,2-butenyl, 2-hexenyl, 10-undecenyl, oleyl, phenyl, methylphenyl,dimethylphenyl, trimethylphenyl, t-butylphenyl, methoxyphenyl,ethoxyphenyl, 3,5-di-t-butyl-4-hydroxyphenyl, benzyl, methylbenzyl,hydroxybenzyl, 3,5-di-t-butyl-4-hydroxybenzyl,2,2,6,6-tetramethylpiperidin-4-yl, 1,2,2,6,6-pentamethylpiperidin-4-yl,1-allyl-2,2,6,6-tetramethylpiperidin-4-yl,1-benzyl-2,2,6,6-tetramethylpiperidin-4-yl and1-acetyl-2,2,6,6-tetramethylpiperidin-4-yl;

for R₇ : ethylene, propylene, trimethylene, tetramethylene,pentamethylene, 2,2-dimethylpropane-1,3-diyl, 2-methylpentane-2,4-diyl,hexamethylene, decamethylene, dodecamethylene, cyclohexylene,cyclohexylenedimethylene, methylenedicyclohexylene, phenylene andxylylene;

for R₁₁, R₁₂, R₁₅, R₁₆, R₁₉, R₂₀, R₂₁, R₂₃, R₂₄, R₂₅ and R₂₆ : ethylene,propylene, trimethylene, tetramethylene, pentamethylene, hexamethyleneand 2-methylpentane-2,4-diyl;

for R₁₃ : hydrogen, methyl, ethyl, propyl, butyl, hexyl, octyl, decyl,dodecyl, cyclopentyl, cyclohexyl, methylcyclohexyl, trimethylcyclohexyl,cyclooctyl, cyclododecyl, 2,2,6,6-tetramethylpiperidin-4-yl,1,2,2,6,6-pentamethylpiperidin-4-yl,1-allyl-2,2,6,6-tetramethylpiperidin-4-yl,1-benzyl-2,2,6,6-tetramethylpiperidin-4-yl and1-acetyl-2,2,6,6-tetramethylpiperidin-4-yl;

for R₁₄, R₁₇, R₁₈ and R₂₂ : hydrogen, methyl, ethyl, propyl, isopropyl,butyl, 2-butyl, isobutyl, t-butyl, hexyl, octyl, 2-octyl, 2-ethylhexyl,decyl, dodecyl, tetradecyl, hexadecyl, octadecyl, cyclopentyl,cyclohexyl, methylcyclohexyl, trimethylcyclohexyl, cyclooctyl,cyclododecyl, benzyl, methylbenzyl, t-butylbenzyl, hydroxybenzyl,3,5-di-t-butyl-4-hydroxybenzyl, 2,2,6,6-tetramethylpiperidin-4-yl,1,2,2,6,6-pentamethylpiperidin-4-yl,1-allyl-2,2,6,6-tetramethylpiperidin-4-yl,1-benzyl-2,2,6,6-tetramethylpiperidin-4-yl and1-acetyl-2,2,6,6-tetramethylpiperidin-4-yl;

for R₂ : methyl, ethyl, propyl, isopropyl, butyl, 2-butyl, isobutyl,t-butyl, hexyl, octyl, 2-ethylhexyl, 1,1,3,3-tetramethylbutyl, decyl,dodecyl, tetradecyl, hexadecyl, octadecyl, cyclohexyl, methylcyclohexyl,trimethylcyclohexyl, cyclooctyl, cyclododecyl, allyl, 2-methallyl,2-butenyl, 2-hexenyl, 10-undecenyl, oleyl, phenyl, methylphenyl,dimethylphenyl, trimethylphenyl, t-butylphenyl, methoxyphenyl,ethoxyphenyl, 3,5-di-t-butyl-4-hydroxyphenyl, benzyl, methylbenzyl,hydroxybenzyl, 3,5-di-t-butyl-4-hydroxybenzyl,2,2,6,6-tetramethylpiperidin-4-yl, 1,2,2,6,6-pentamethylpiperidin-4-yl,1-allyl-2,2,6,6-tetramethylpiperidin-4-yl,1-benzyl-2,2,6,6-tetramethylpiperidin-4-yl and1-acetyl-2,2,6,6-tetramethylpiperidin-4-yl, or, if m is 1 and R₁ is agroup ##STR14## R₂ can be a group of the formula (III) is which R₂₇ is,for example, ethylene, propylene, trimethylene, tetramethylene,pentamethylene, hexamethylene, 2,2-dimethylpropane-1,3-diyl,2-methylpentane-2,4-di-yl, decamethylene, dodecamethylene,cyclohexylene, cyclohexylenedimethylene, methylenedicyclohexylene or oneof the groups R₂₇ ', R₂₇ ' and R₂₇ "' in which R₂₈ and R₂₉ can bemethyl, ethyl, propyl or butyl and R₃ and R₅ are as defined above.

If R₁ is a heterocyclic group and if m=1, preferred examples are:pyrrolidinyl, piperidino, morpholino, 2,6-di-methylmorpholino,4-methylpiperazin-1-yl, 3,3,5,5-tetramethylpiperazin-1-yl,hexahydroazepin-1-yl or a radical ##STR15## in which q is an integerfrom 3 to 11; if m=2, preferred examples are: ##STR16## if m=3, R₁ canbe a hexahydro-1,3,5-triazine-1,3,5-triyl group and if m=4, R₁ can beone of the following groups: ##STR17## Those compounds of the formula(I) are preferred in which, if m=1, R₁ is a group ##STR18## in which R₃and R₄ are identical or different and are hydrogen, C₁ -C₁₂ -alkyl, C₆-C₁₂ -cycloalkyl, allyl, phenyl, benzyl or a group of the formula (II)in which R₅ is hydrogen, methyl, allyl, benzyl or acetyl, or R₁ is aheterocyclic radical selected from the group consisting of piperidino,morpholino and hexahydroazepin-1-yl; or if m is 2, R₁ is a group##STR19## in which R₆ and R₈ are identical or different and arehydrogen, C₁ -C₁₂ -alkyl, C₆ -C₉ -cycloalkyl or a group of the formula(II) and R₇ is C₂ -C₁₂ -alkylene or a group --R₁₁ --X--(R₁₂ --X--_(n)R₁₁ -- in which R₁₁ and R₁₂ are identical or different and are C₂ -C₆-alkylene, X is --O-- and n is zero, 1 or 2, or R₁ ispiperazine-1,4-diyl or 5,5,7-trimethylhomopiperazine-1,4-diyl; or if mis 3, R₁ is a group ##STR20## in which R₁₄ and R₁₇ are identical ordifferent and are hydrogen, C₁ -C₈ -alkyl, C₆ -C₉ -cycloalkyl or a groupof the formula (II) and R₁₅ and R₁₆ are identical or different and areC₂ -C₆ -alkylene, or R₁ is a hexahydro-1,3,5-triazine-1,3,5-triyl group;or if m is 4, R₁ is a group ##STR21## in which R₁₈ and R₂₂ are identicalor different and are hydrogen, C₁ -C₈ -alkyl, C₆ -C₉ -cycloalkyl or agroup of the formula (II) and R₁₉, R₂₀ and R₂₁ are identical ordifferent and are C₂ --C₆ -alkylene, or R₁ is a group ##STR22## R₂ is C₁-C₁₂ -alkyl, C₆ -C₉ -cycloalkyl, allyl, phenyl, benzyl or a group of theformula (II) or, if m is 1 and R₁ is a group ##STR23## with R₃ and R₅being as defined above, R₂ additionally is a group of the formula (III)in which R₂₇ is C₂ -C₆ -alkylene, C₆ -C₁₂ -cycloalkylene or one of thegroups R₂₇ ', R₂₇ " and R₂₇ '" and R₂₇ '" wherein R₂₈ is hydrogen ormethyl, R₂₉ is methyl, ethyl or a group ##STR24## in which R₃ and R₅ areas defined above and p is 1, with the proviso that at least one group ofthe formula (II) is present in R₁ or R₂.

Those compounds of the formula (I) are particularly preferred in which mis 1 or 2 and, if m is 1, R₁ is a group ##STR25## in which R₃ ishydrogen, C₁ -C₈ -alkyl, cyclohexyl, 2,2,6,6-tetramethylpiperidin-4-ylor 1,2,2,6,6-pentamethylpiperidin-4-yl and R₄ is2,2,6,6-tetramethylpiperidin-4-yl or1,2,2,6,6-pentamethylpiperidin-4-yl, or, if m is 2, R₁ is a group##STR26## in which R₆ and R₈ are 2,2,6,6-tetramethylpiperidin-4-yl or1,2,2,6,6-pentamethylpiperidin-4-yl and R₇ is C₂ -C₆ -alkylene, or R₁ ispiperazine-1,4-diyl or 5,5,7-trimethylhomopiperazine-1,4-diyl, R₂ is2,2,6,6-tetramethylpiperidin-4-yl or1,2,2,6,6-pentamethylpiperidin-4-yl, or if m is 1 and R₁ is a group##STR27## R₂ additionally is one of the groups ##STR28## in which R₃ isas defined above and R₅ is hydrogen or methyl.

Those compounds of the formula (I) wherein m is 1, constitute apreferred embodiment of the invention.

Compounds of the formula (I) in which m is 2 are particularly preferred.

The novel compounds according to the present invention are prepared byvarious processes in accordance with their chemical characteristics.

In particular, if R₂ is a group R₂ ' defined as C₁ -C₁₈ -alkyl,unsubstituted or substituted C₅ -C₁₈ -cycloalkyl, C₃ -C₁₈ -alkenyl,unsubstituted or substituted C₆ -C₁₈ -aryl, unsubstituted or substitutedC₇ -C₁₈ -aralkyl or a group of the formula (II), the compounds of theformula (I) can be prepared by reacting a compound of the formula (IV)

    R.sub.1 (H).sub.m                                          (IV),

in which R₁ and m are as defined above, with a chlorooxoacetate of theformula (V) ##STR29## in which R'₂ is as defined above. A variant ofthis process is the reaction of a chlorooxoacetamide of the formula (VI)with an alcohol of the formula (VII) ##STR30## in which R₁, m and R'₂are as defined above.

If m is 1, R₁ is ##STR31## and R₂ is a group of the formula (III), thecompounds of the formula (I) can be prepared by reacting achlorooxoacetamide of the formula (VIII) ##STR32## with a compound ofthe formula (IX), (X) or (XI) ##STR33## in which R₃₀ is C₂ -C₁₂-alkylene, C₆ -C₁₈ -cycloalkylene or a group ##STR34## with R₂₈ being asdefined above, and p is 1 to 4.

An alternative for this last process is the reaction of a compound ofthe formula (XII) ##STR35## in which R₃ and R₅ are as defined above andR₂ " is C₁ -C₄ -alkyl, with a compound of the formula (IX), (X) or (XI).

If R₂ is a group R₂ '" defined as C₄ -C₁₈ -alkyl, unsubstituted orsubstituted C₅ -C₁₈ -cycloalkyl, C₃ -C₁₈ -alkenyl, unsubstituted orsubstituted C₆ -C₁₈ -aryl, unsubstituted or substituted C₇ -C₁₈ -aralkylor a group of the formula (II), the compounds of the formula (I) canalso be prepared by reacting a compound of the formula (XIII) ##STR36##in which R₁, m and R₂ " are as defined above, with an alcohol of theformula (XIV)

    R.sub.2 '"--OH                                             (XIV)

in which R₂ '" is as defined above, with the proviso that R₂ " is C₁ -C₃-alkyl if R₂ '" is C₄ -alkyl.

The reactions with chlorooxoacetates (V) and with thechlorooxoacetamides (VI) or (VIII) can be carried out in an inertsolvent such as a hydrocarbon, for example n-hexane, or a chlorinatedhydrocarbon, for example dichloromethane or dichloroethane, in astoichiometric molar ratio of the reagents or with an excess of up to20% of theory of the monofunctional reagents, neutralising thehydrochloric acid liberated in the reactions with an inorganic base,such as sodium or potassium hydroxide or carbonate, in a quantity almostequivalent to the acid, and operating at a temperature between -30° C.and 100 C., preferably -10° C. to 50° C. If the group of the formula(II) is present, the intermediates of the formulae (V), (VI) and (VIII)are preferably employed in the form of the hydrochlorides. The reactionswith the compounds (XII) and (XIII) can be carried out without a solventor in the presence of an inert solvent as defined above, in astoichiometric molar ratio of the reagents or with an excess of up to50% of theory of the monofunctional reagents, at temperatures between100° and 250° C., preferably 120° C. and 200° C., in the presence of atransesterification catalyst, such as an alkali metal or an amide,alcoholate or hydride thereof, or in the presence of titanium (IV)alkoxides.

The intermediates employed for the preparation of the compounds of theformula (I) can be prepared by known processes. In particular, thechlorooxoacetates of the formula (V) can be prepared by reacting oxalylchloride with an alcohol of the formula (VII), the chlorooxoacetamides(VI) can be prepared by reacting oxalyl chloride with a compound of theformula (IV) and the chlorooxoacetamides (VIII) can be prepared fromoxalyl chloride and a compound of the formula (XV) ##STR37## Thecompounds (XII) and (XIII) can be prepared by reacting a compound of theformula (XV) or (IV), respectively, with a C₁ -C₄ -alkylchlorooxoacetate or with a C₁ -C₄ -alkyl oxalate.

The intermediates (V), (VI), (VIII), (XII) or (XIII) can be employeddirectly in the preparation of the compounds of the formula (I), withoutisolating them from the reaction mixture or after separation orpurification.

In order to illustrate the present invention more clearly, severalexamples of the preparation of the compounds of the formula (I) aredescribed below; these examples are given by way of illustration onlyand do not imply any restriction.

EXAMPLE 1

Preparation of the compound ##STR38## A solution of 75.1 g (0.55 mol) ofethyl chlorooxoacetate in 100 ml of dichloromethane is added slowly to asolution, cooled to 0° C., of 92 g (0.5 mol) of4-ethylamino-2,2,6,6-tetramethylpiperidine in 500 ml of dichloromethane.

The rate of addition is controlled such that the temperature remainsbetween 0° and 5° C.

The solution is stirred for 3 hours at 10°-15° C. and then cooled to 0°C.

A solution of 22 g (0.55 mol) of sodium hydroxide in 60 ml of water isthen added slowly, while maintaining the temperature between 0° and 5°C.

After the end of the addition, the mixture is stirred for 30 minutes at10°-15° C. The aqueous phase is separated off and the organic phase iswashed with water, dried and evaporated.

The residue is crystallised from n-hexane.

This gives 126.8 g of a product of melting point 53°-54° C.

Analysis for C₁₅ H₂₈ N₂ O₃ : Calculated: C 63.35%; H 9.91%; N 9.85%:Found: C 63.60%; H 9.88%; N 9.95%.

EXAMPLES 2-5

Repeating the procedure described in Example 1, but employing theappropriate intermediates, the following compounds of the formula (I)are prepared.

    __________________________________________________________________________    Example No.                                                                          Product                        Melting point (°C.)              __________________________________________________________________________            ##STR39##                     150.9                                   3                                                                                     ##STR40##                     131.7                                   4                                                                                     ##STR41##                     132.9                                   5                                                                                     ##STR42##                     190.9                                   __________________________________________________________________________

EXAMPLE 6

Preparation of the compound ##STR43##

(a) Preparation of 1,2,2,6,6-pentamethylpiperidin-4-yl chlorooxoacetatehydrochloride:

A solution of 137 g (0.8 mol) of4-hydroxy-1,2,2,6,6-pentamethylpiperidine in 2000 ml of n-hexane isslowly added to a solution, cooled to -30° C., of 203.2 g (1.6 mol) ofoxalyl chloride in 2300 ml of n-hexane, while maintaining the abovetemperature.

The mixture is then stirred for 12 hours, while allowing the temperatureto rise gradually to about 20° C.

The precipitate obtained is separated off by filtration and dried at 25°C. in vacuo (26.7 mbar).

This gives 235 g of product which can be used directly for thesubsequent reactions.

Analysis for C₁₂ H₂₁ Cl₂ NO₃ : Calculated: Cl 23.77%: Found: Cl 23.58%.

(b) Preparation of 1,2,2,6,6-pentamethylpiperidin-4-ylN-2,2,6,6-tetramethylpiperidin-4-yl-aminooxoacetate:

A solution of 18.7 g (0.12 mol) of 4-amino-2,2,6,6-tetramethylpiperidinein 40 ml of dichloromethane is added slowly to a solution, cooled toabout 0° C., of 29.8 g (0.1 mol) of 1,2,2,6,6-pentamethylpiperidin-4-ylchlorooxoacetate hydrochloride in 100 ml of dichloromethane, whilemaintaining the temperature at 0°-5° C.

The mixture is stirred for 1 hour at 0°-5° C. and for 4 hours at ambienttemperature.

After cooling again to 0°-5° C., a solution 10 g (0.25 mol) of sodiumhydroxide in 30 ml of water is added. After the end of the addition, themixture is stirred for 1 hour at 0°-5° C. and for 1 hour at ambienttemperature.

The organic phase is separated off, washed with water, dried andevaporated.

The residue is crystallised from n-hexane.

This gives 34.7 g of product of melting point 142°-143° C.

Analysis for C₂₁ H₃₉ N₃ O₃ : Calculated: C 66.10%; H 10.30%; N 11.01%:Found: C 66.79%; H 10.34%; N 11.12%.

EXAMPLE 7

Preparation of the compound: ##STR44##

(a) Preparation of 2,2,6,6-tetramethylpiperidin-4-yl chlorooxoacetatehydrochloride:

67.1 g (0.52 mol) of oxalyl chloride are added to a mixture of 51.1 g(0.26 mol) of 4-hydroxy-2,2,6,6-tetramethylpiperidine hydrochloride and500 ml of dichloroethane, and the mixture is heated under reflux for 6hours.

The solution thus obtained is evaporated in vacuo (26.7 mbar) and theresidue (73.5 g) can be employed directly for the subsequent reactions.

Analysis for C₁₁ H₁₉ Cl₂ NO₃ : Calculated: Cl 24.95%: Found: Cl 24.88%.

(b) Preparation of 2,2,6,6-tetramethylpiperidin-4-ylN-methyl-N-2,2,6,6-tetramethylpiperidin-4-yl-aminooxoacetate:

A solution of 20.4 g (0.12 mol) of4-methylamino-2,2,6,6-tetramethylpiperidine in 40 ml of dichloromethaneis added slowly to a solution, cooled to about 0° C., of 28.4 g (0.1mol) of 2,2,6,6-tetramethylpiperidin-4-yl chlorooxoacetate hydrochloridein 100 ml of dichloromethane, while maintaining the temperature at 0° C.

The mixture is stirred for 1 hour 0°-5° C. and for 4 hours at ambienttemperature. After cooling again to about 0° C., a solution of 10 g(0.25 mol) of sodium hydroxide in 30 ml of water is added. After the endof the addition, the mixture is stirred for 1 hour at 0°-5° C. and for 1hour at ambient temperature.

The organic phase is separated off, washed with water, dried andevaporated.

The residue is crystallised from n-hexane.

This gives 28.5 g of product of melting point 97°-98° C.

Analysis for C₂₁ H₃₉ N₃ O₃ : Calculated: C 66.11%; H 10.30%; N 11.01%:Found: C 66.09%; H 10.28%; N 10.88%.

EXAMPLES 8-24

Repeating the procedures described in Examples 6 and 7, but employingthe appropriate intermediates, the following compounds of the formula(I) are prepared.

    __________________________________________________________________________    Example No.                                                                          Product                                           m.p.                 __________________________________________________________________________                                                             (°C.)          8                                                                                    ##STR45##                                        80-81                 9                                                                                    ##STR46##                                        103-104              10                                                                                    ##STR47##                                        88-89                11                                                                                    ##STR48##                                        resin                12                                                                                    ##STR49##                                        147                  13                                                                                    ##STR50##                                        178-179              14                                                                                    ##STR51##                                        Oil                  15                                                                                    ##STR52##                                        158-159              16                                                                                    ##STR53##                                        217-218              17                                                                                    ##STR54##                                        227-228              18                                                                                    ##STR55##                                        149-150              19                                                                                    ##STR56##                                        170-171              20                                                                                    ##STR57##                                        116-117              21                                                                                    ##STR58##                                        210-211              22                                                                                    ##STR59##                                        224-225              23                                                                                    ##STR60##                                        121-122              24                                                                                    ##STR61##                                        136-137              __________________________________________________________________________

EXAMPLE 25

Preparation of the compound: ##STR62## A solution of 39.1 g (0.31 mol)of oxalyl chloride in 50 ml of dichloroethane is added slowly to asolution, cooled to 0° C., of 39.6 g (0.15 mol) of4-ethylamino-2,2,6,6-tetramethylpiperidine dihydrochloride in 250 ml ofdichloroethane, while maintaining the temperature between 0° and 10° C.

The mixture is heated for 4 hours under reflux, and the solvent and theexcess oxalyl chloride are distilled off in vacuo (26.7 mbar).

The crude product thus obtained, consisting ofN-ethyl-N-(2,2,6,6-tetramethylpiperidin-4-yl)-chlorooxoacetamidehydrochloride, is dissolved in 200 ml of dichloroethane.

14.1 g (0.07 mol) of1-(2-hydroxyethyl)-4-hydroxy-2,2,6,6-tetramethylpiperidine are added tothe solution thus obtained at a temperature of 15°-20° C.

The mixture is heated under reflux for 6 hours. After cooling again to0°-5° C., a solution of 13.2 g (0.33 mol) of sodium hydroxide in 50 mlof water is added.

The mixture is stirred for 1 hour at ambient temperature.

The phases are separated. The organic phase is washed with water, driedand evaporated.

This gives 40.5 g of product of melting point 141°-142° C.

Analysis for C₃₇ H₆₇ N₅ O₆ : Calculated: C 65.55%; H 9.96%; N 10.33%:Found: C 65.19%; H 9.97%; N 10.27%.

EXAMPLE 26

Preparation of the compound: ##STR63## 4.05 g (0.045 mol) of1,4-butanediol and 1 ml of titanium tetraisopropylate are added to 31.2g (0.1 mol) of ethylN-butyl-N-2,2,6,6-tetramethylpiperidin-4-yl-aminooxoacetate preparedfrom 4-butylamino-2,2,6,6-tetramethylpiperidine and ethylchlorooxoacetate by the procedure described in Example 1.

The mixture is heated for 4 hours at 140°-150° C. under a gentlenitrogen stream with elimination of the ethanol of reaction (5.3 ml) andthen for 1 hour at 150° C. under 6.67 mbar.

After cooling, the reaction mixture is dissolved in 100 ml ofdichloroethane, and the solution is washed with water, dried andevaporated.

The residue is crystallised from n-hexane. This gives 17.3 g of productof melting point 64° C.

Analysis for C₃₄ H₆₂ N₄ O₆ : Calculated: C 65.56%; H 10.03%; N 8.99%:Found: C 65.74%; H 10.11%; N 8.98%.

EXAMPLES 27-33

Repeating the procedure of Example 26, but employing the reagentsindicated, the following compounds of formula (I) are prepared.

    __________________________________________________________________________                                                              m.p.                Ex. No.                                                                            Reagents             Product                         (°C.)        __________________________________________________________________________    27                                                                                  ##STR64##                                                                                          ##STR65##                      resin               28                                                                                  ##STR66##                                                                                          ##STR67##                      56-57                     ##STR68##                                                               29                                                                                  ##STR69##                                                                                          ##STR70##                      88-89               30                                                                                  ##STR71##                                                                                          ##STR72##                      89-90               31                                                                                  ##STR73##                                                                                          ##STR74##                      resin               32                                                                                  ##STR75##                                                                                          ##STR76##                      resin               33                                                                                  ##STR77##                                                                                          ##STR78##                      resin               __________________________________________________________________________

As mentioned at the outset, the compounds of the formula (I) are veryeffective in improving the light stability, heat stability and oxidationstability of organic material, especially synthetic polymers, forexample high-density and low-density polyethylene, polypropylene,ethylene/propylene copolymers, ethylene/vinyl acetate copolymers,polybutadiene, polyisoprene, polystyrene, butadiene/styrene copolymers,vinyl chloride/vinylidene chloride polymers and copolymers,polyoxymethylene, polyphenylene oxide, polyurethanes, saturated andunsaturated polyesters, polyamides, polycarbonates, polyacrylates, alkydresins and epoxide resins.

A further embodiment of the present invention is an organic materialcontaining a compound of the formula (I). The organic material ispreferably a synthetic polymer. Polyethylene and polypropylene areparticularly preferred.

The compounds of the formula (I) can be mixed with organic material, forexample synthetic polymers, in various proportions depending on thenature of the polymer, the end use and the presence of other additives.

In general, it is advantageous to employ from 0.01 to 5% by weight ofthe compounds of the formula (I), relative to the weight of thepolymers, preferably from 0.05 to 1%.

The compounds of the formula (I) can be incorporated into the polymericmaterials by various processes, such as dry blending in the form ofpowders, or wet mixing in the form of solutions or suspensions, or inthe form of a masterbatch; in these operations, the polymer can beemployed in the form of powder or granules or in the form of a solution,a suspension or a latex.

The organic material stabilised with the products of the formula (I) canbe used for the preparation of moulded articles, films, tapes, fibres,monofilaments, surface-coatings and the like.

If desired, other additives, for example antioxidants, ultravioletabsorbers, nickel stabilisers, pigments, fillers, plasticisers,antistatic agents, flameproofing agents, lubricants, corrosioninhibitors and metal deactivators, can be added to the mixtures of thecompounds of the formula (I) with the polymers. Examples of additiveswhich can be mixed with the compounds of the formula (I) are, inparticular:

1. Antioxidants

1.1. Alkylated monophenols, for example,

2,6-di-tert.butyl-4-methylphenol

2-tert.butyl-4,6-dimethylphenol

2,6-di-tert.butyl-4-ethylphenol

2,6-di-tert.butyl-4-n-butylphenol

2,6-di-tert.butyl-4-i-butylphenol

2,6-di-cyclopentyl-4-methylphenol

2-(α-methylcyclohexyl)-4,6-dimethylphenol

2,6-di-octadecyl-4-methylphenol

2,4,6-tri-cyclohexylphenol

2,6-di-tert.butyl-4-methoxymethylphenol

1.2. Alkylated hydroquinones, for example,

2,6-di-tert.butyl-4-methoxyphenol

2,5-di-tert.butyl-hydroquinone

2,5-di-tert.amyl-hydroquinone

2,6-diphenyl-4-octadecyloxyphenol

1.3. Hydroxylated thiodiphenyl ethers, for example,

2,2'-thio-bis-(6-tert.butyl-4-methylphenol)

2,2'-thio-bis-(4-octylphenol)

4,4'-thio-bis-(6-tert.butyl-3-methylphenol)

4,4'-thio-bis-(6-tert.butyl-2-methylphenol)

1.4. Alkyliden-bisphenols, for example,

2,2'-methylene-bis-(6-tert.butyl-4-methylphenol)

2,2'-methylene-bis-(6-tert.butyl-4-ethylphenol)

2,2'-methylene-bis-[4-methyl-6-(α-methylcyclohexyl)-phenol]

2,2'-methylene-bis-(4-methyl-6-cyclohexylphenol)

2,2'-methylene-bis-(6-nonyl-4-methylphenol)

2,2'-methylene-bis-[6-(α-methylbenzyl)-4-nonylphenol]

2,2'-methylene-bis-[6-(α,α-dimethylbenzyl)-4-nonylphenol]

2,2'-methylene-bis-(4,6-di-tert.butylphenol)

2,2'-ethylidene-bis-(4,6-di-tert.butylphenol)

2,2'-ethylidene-bis-(6-tert.butyl-4-isobutylphenol)

4,4'-methylene-bis-(2,6-di-tert.butylphenol)

4,4'-methylene-bis-(6-tert.butyl-2-methylphenol)

1,1-bis-(5-tert.butyl-4-hydroxy-2-methylphenyl)-butane

2,6-bis-(3-tert.butyl-5-methyl-2-hydroxybenzyl)-4-methylphenol

1,1,3-tris-(5-tert.butyl-4-hydroxy-2-methylphenyl)-butane

1,1-bis-(5-tert.butyl-4-hydroxy-2-methylphenyl)-3-n-dodecylmercaptobutane

ethylenglycol-bis-[3,3-bis-(3'-tert.butyl-4'-hydroxyphenyl)-butyrate]

bis-(3-tert.butyl-4-hydroxy-5-methylphenyl)-dicyclopentadiene

bis-[2-(3'-tert.butyl-2'-hydroxy-5'-methyl-benzyl)-6-tert.butyl-4-methylphenyl]-terephthalate.

1.5. Benzylcompounds, for example,

1,3,5-tri-(3,5-di-tert.butyl-4-hydroxybenzyl)-2,4,6-trimethylbenzene

bis-(3,5-di-tert.butyl-4-hydroxybenzyl)sulfide

3,5-di-tert.butyl-4-hydroxybenzylmercaptoacetic acid isooctyl ester

bis-(4-tert.butyl-3-hydroxy-2,6-dimethylbenzyl)dithiol terephthalate

1,3,5-tris-(3,5-di-tert.butyl-4-hydroxybenzyl)isocyanurate

1,3,5tris-(4-tert.butyl-3-hydroxy-2,6-dimethylbenzyl)isocyanurate

3,5-di-tert.butyl-4-hydroxybenzyl-phosphonic acid dioctadecyl ester

3,5-di-tert.butyl-4-hydroxybenzyl-phosphonic acid monoethyl estercalcium salt

1.6. Acylaminophenols, for example,

anilide of 4-hydroxy-lauric acid

anilide of 4-hydroxy-stearic acid

2,4-bis-octylmercapto-6-(3,5-tert.butyl-4-hydroxyanilino)-s-triazine

octyl-N-(3,5-di-tert.butyl-4-hydroxyphenyl)-carbamate

1.7. Esters of β-(3,5-di-tert.butyl-4-hydroxyphenyl)-propionic acid withmonohydric or polyhydric alcohols, for example,

methanol

octadecanol

1,6-hexanediol

neopentylglycol

thiodiethyleneglycol

diethyleneglycol

triethyleneglycol

pentaerythritol

tris-(hydroxyethyl)isocyanurate

N,N'-bis(hydroxyethyl)oxalic

acid diamide

1.8. Ester of β-(5-tert.butyl-4-hydroxy-3-methylphenyl)propionic acidwith monohydric or polyhydric alcohols, for example,

methanol

octadecanol

1,6-hexanediol

neopentylglycol

thiodiethyleneglycol

diethyleneglycol

triethyleneglycol

pentaerytritol

tris-(hydroxyethyl)isocyanurate

N,N'-bis(hydroxyethyl)oxalic

acid diamide

1.9. Amides of β-(3,5-di-tert.butyl-4-hydroxyphenyl)-propionic acid forexample,

N,N'-bis-(3,5-di-tert.butyl-4-hydroxyphenylpropionyl)-hexamethylendiamine

N,N'-bis-(3,5-di-tert.butyl-4-hydroxyphenylpropionyl)-trimethylendiamine

N,N'-bis-(3,5-di-tert.butyl-4-hydroxyphenylpropionyl)-hydrazine

2. UV absorbers and light stabilisers

2.1. 2-(2'-Hydroxyphenyl)-benzotriazoles, for example, the 5'-methyl-,3',5'-di-tert.butyl-, 5'-tert.butyl-, 5'-(1,1,3,3-tetramethylbutyl)-,5-chloro-3',5'-di-tert.butyl-, 5-chloro-3'-tert.butyl-5'-methyl-,3'-sec.butyl-5'-tert.butyl-, 4'-octoxy-, 3',5'-di-tert.amyl-,3',5'-bis-(α,α-dimethylbenzyl)-derivative.

2.2. 2-Hydroxy-benzophenones, for example, the 4-hydroxy-, 4-methoxy-,4-octoxy, 4-decyloxy-, 4-dodecyloxy-, 4-benzyloxy, 4,2',4'-trihydroxy-and 2'-hydroxy-4,4'-dimethoxyderivative.

2.3. Esters of optionally substituted benzoic acids for example, phenylsalicylate, 4-tert.butyl-phenyl salicylate, octylphenyl salicylate,dibenzoylresorcinol, bis-(4-tert.butylbenzoyl)-resorcinol,benzoylresorcinol, 3,5-di-tert.-butyl-4-hydroxybenzoic acid2,4-di-tert.butyl-phenyl ester and 3,5-di-tert.-butyl-4-hydroxybenzoicacid hexadecyl ester.

2.4. Acrylates, for example, α-cyano-β,β-diphenylacrylic acid ethylester of isooctyl ester, α-carbomethoxy-cinnamic acid methyl ester,α-cyano-β-methyl-p-methoxycinnamic acid methyl ester or butyl ester,α-carbomethoxy-p-methoxycinnamic acid methyl ester,N-(β-carbomethoxy-β-cyanovinyl)-2-methylindoline.

2.5 Nickel compounds, for example, nickel complexes of2,2'-thio-bis-[4-(1,1,3,3-tetramethylbutyl)-phenol], such as the 1:1 or1:2 complex, optionally with additional ligands such as n-butylamine,triethanolamine or N-cyclohexyl-di-ethanolamine, nickeldibutyldithiocarbamate, nickel salts of4-hydroxy-3,5-di-tert.butylbenzylphosphonic acid monoalkyl esters, suchas of the methyl, ethyl or butyl ester, nickel complexes of ketoximessuch as of 2-hydroxy-4-methyl-phenyl undecyl ketonoxime, nickelcomplexes of 1-phenyl-4-lauroyl-5-hydroxypyrazole, optionally withadditional ligands.

2.6. Sterically hindered amines, for example,

bis-(2,2,6,6-tetramethylpiperidyl)sebacate

bis-(1,2,2,6,6-pentamethylpiperidyl)sebacate

n-butyl-3,5-di-tert.butyl-4-hydroxybenzyl malonic acidbis(1,2,2,6,6-pentamethylpiperidyl)ester, condensation product of1-hydroxyethyl-2,2,6,6-tetramethyl-4-hydroxypiperidine and succinicacid, condensation product ofN,N'-bis-(2,2,6,6-tetramethylpiperidyl)-hexamethylendiamine and4-tert.octylamino-2,6-dichloro-1,3,5-s-triazine,tris-(2,2,6,6-tetramethylpiperidyl)nitrilotriacetate,tetrakis-(2,2,6,6-tetramethyl-4-piperidyl)1,2,3,4-butanetetracarboxylate,1,1'(1,2-ethanediyl)-bis-(3,3,5,5-tetramethylpiperazinone).

2.7. Oxalic acid diamides, for example, 4,4'-di-octyloxy oxanilide,2,2'-di-octyloxy-5,5'-di-tert.butyl oxanilide,2,2'-di-dodecyloxy-5,5'-di-tert.butyl oxanilide, 2-ethoxy-2'-ethyloxanilide, N,N'-bis-(3-dimethylaminopropyl)-oxalamide,2-ethoxy-5-tert.butyl-2'-ethyloxanilide and its mixture with2-ethoxy-2'-ethyl-5,4'-di-tert.butyloxanilide and mixtures of ortho-andpara-methoxy- as well as of o- and p-ethoxy-disubstituted oxanilides.

3. Metal deactivators, for example, N,N'-diphenyl oxalic acid diamideN-salicylal-N'-salicyloylhydrazine, N,N'-bis-(salicyloyl)-hydrazine,N,N'-bis-(3,5-di-tert.butyl-4-hydroxyphenylpropionyl)-hydrazine,3-salicyloylamino-1,2,4-triazole, bis-(benzylidene)oxalic aciddihydrazide.

4. Phosphites and phosphonites, for example, triphenyl phosphite,diphenylalkyl phosphites, phenyldialkyl phosphites,tri-(nonylphenyl)phosphite, trilauryl phosphite, trioctadecyl phosphite,di-stearyl pentaerythritol diphosphite,tris-(2,4-di-tert.butylphenyl)phosphite, di-isodecyl pentaerythritoldiphosphite, di-(2,4-di-tert.butylphenyl)pentaerythritol diphosphite,tristearyl-sorbitol triphosphite, tetrakis-(2,4-di-tert.butylphenyl)4,4'-biphenylene diphosphonite.

5. Compounds which destroy peroxide, for example, esters ofβ-thiodipropionic acid, for example the lauryl, stearyl, myristyl ortridecyl esters, mercaptobenzimidazole or the zinc salt of2-mercaptobenzimidazole, zinc-dibutyl-dithiocarbamate,dioctadecyldisulfide, pentaerythritoltetrakis-(β-dodecylmercapto)-propionate.

6. Polyamide stabilisers, for example, copper salts in combination withiodides and/or phosphorus compounds and salts of divalent manganese.

7. Basic co-stabilisers, for example, melamine, polyvinylpyrrolidone,dicyandiamide, triallyl cyanurate, urea derivatives, hydrazinederivatives, amines, polyamides, polyurethanes, alkali metal salts andalkaline earth metal salts of higher fatty acids for example Castearate, Zn stearate, Mg stearate, Na ricinoleate and K palmitate,antimony pyrocatecholate or zinc pyrocatecholate.

8. Nucleating agents, for example, 4-tert.butyl benzoic acid, adipicacid, diphenylacetic acid.

9. Fillers and reinforcing agents, for example, calcium carbonate,silicates, glass fibres, asbestos, talc, kaolin, mica, barium sulfate,metal oxides and hydroxydes, carbon black, graphite.

10. Other additives, for example, plasticisers, lubricants, emulsifiers,pigments, optical brighteners, flameproofing, agents, antistatic agentsand blowing agents.

The efficiency, as stabilisers, of the products prepared according tothe present invention is illustrated by the examples which follow, inwhich some products obtained in the preparation examples are used forstabilising polypropylene tapes and sheets.

EXAMPLE 34

2 g of each of the compounds indicated in Table 1, 1 g ofpentaerythritol tetrakis-3-(3,5-di-t-butyl-4-hydroxy-phenyl)-propionateand 1 g of calcium stearate are mixed in a powder mixer with 1,000 g ofpolypropylene powder of melt index 3 (® Propathene HF 22, a product ofImperial Chemical Industries).

The mixtures obtained are extruded at a temperature of 180°-220° C., togive polymer granules which are then converted into stretched tapes of50μ thickness and 2.5 mm width, under the following working conditions:

Extruder temperature: 220°-240° C.

Head temperature: 240° C.

Stretch ratio: 1:6

The tapes thus prepared are exposed, mounted on a white card, in a 65 WRmodel Weather-Ometer (ASTM G 27-70), with a black panel temperature of63° C.

The residual tenacity is measured on samples, taken after various timesof exposure to light, by means of a constant-speed tensometer; theexposure time in hours (T₅₀) needed to halve the initial tenacity isthen calculated.

For comparison, tapes prepared under the same conditions as indicatedabove, but without the addition of the compounds of the invention, arealso exposed. The results obtained are shown in Table 1.

                  TABLE 1                                                         ______________________________________                                        Stabiliser         T.sub.50 (hours)                                           ______________________________________                                        without stabiliser   216                                                      Compound of Example 2                                                                            2,160                                                      Compound of Example 3                                                                            1,780                                                      Compound of Example 7                                                                            1,920                                                      Compound of Example 8                                                                            2,420                                                      Compound of Example 9                                                                            1,910                                                      Compound of Example 10                                                                           2,800                                                      Compound of Example 11                                                                           3,390                                                      Compound of Example 13                                                                           3,100                                                      Compound of Example 14                                                                           2,150                                                      Compound of Example 17                                                                           1,900                                                      Compound of Example 18                                                                           2,000                                                      Compound of Example 19                                                                           2,200                                                      Compound of Example 20                                                                           2,490                                                      Compound of Example 21                                                                           2,410                                                      Compound of Example 22                                                                           2,350                                                      Compound of Example 24                                                                           2,210                                                      Compound of Example 27                                                                           1,740                                                      Compound of Example 28                                                                           1,770                                                      Compound of Example 29                                                                           2,060                                                      Compound of Example 30                                                                           2,050                                                      ______________________________________                                    

EXAMPLE 35

1.0 g of each of the products indicated in Table 2, 1 g ofpentaerythritol tetrakis-3-(3,5-di-t-butyl-4-hydroxyphenyl)propionate, 1g of calcium stearate, 1 g of blue phtalocyanine and 1,000 g ofpolypropylene powder of melt index 3 (® Propathene HF 22, product ofImperial Chemical Industries) are intimately mixed in a slow mixer.

The mixtures obtained are extruded at a temperature of 200°-220° C. togive polymer granules which are then converted into 2 mm thick sheets bydie extrusion at 250° C.

The sheets thus obtained are exposed in a 65 WR model Weather-Ometer(ASTM G 27-70), with a black panel temperature of 63° C., up to theonset of surface embrittlement (chalking).

For comparison, a polypropylene sheet prepared under the same conditionsas indicated above, but without the addition of the compounds of theinvention, is also exposed.

The exposure time (in hours) required for such an onset of embrittlementis indicated in Table 2.

                  TABLE 2                                                         ______________________________________                                                         Surface embrittlement                                        Stabiliser       time (hours)                                                 ______________________________________                                        Without stabiliser                                                                               510                                                        Compound of Example 2                                                                          2,300                                                        Compound of Example 7                                                                          2,700                                                        Compound of Example 8                                                                          2,500                                                        Compound of Example 9                                                                          3,000                                                        Compound of Example 10                                                                         2,650                                                        Compound of Example 11                                                                         3,500                                                        Compound of Example 20                                                                         2,700                                                        Compound of Example 21                                                                         2,400                                                        Compound of Example 22                                                                         2,490                                                        Compound of Example 28                                                                         3,000                                                        Compound of Example 30                                                                         2,200                                                        ______________________________________                                    

What we claim is:
 1. A composition of matter comprising an organicmaterial subject to oxidative, thermal or actinic degradation stabilizedwith an effective stabilizing amount of a compound of the formula##STR79## wherein m is an integer from 1 to 4 and, if m=1, R₁ is a group##STR80## in which R₃ and R₄ are identical or different and arehydrogen, C₁ -C₁₈ -alkyl, C₂ -C₆ -alkyl substituted by C₁ -C₁₈ -alkoxyor by C₂ -C₁₈ -dialkylamino, C₅ -C₁₈ -cycloalkyl, C₃ -C₁₈ -alkenyl, C₆-C₁₈ -aryl unsubstituted or substituted by C₁ -C₁₂ -alkoxy, by C₁ -C₁₂-alkyl and/or by --OH, C₇ -C₁₈ -aralkyl unsubstituted or substituted byC₁ -C₁₂ -alkyl and/or by --OH or are a group of the formula (II)##STR81## wherein R₅ is hydrogen, O., cyanomethyl, C₁ -C₁₂ -alkyl, C₃-C₁₂ -alkenyl or C₃ -C₁₂ -alkynyl, C₇ -C₁₂ -aralkyl unsubstituted orsubstituted by C₁ -C₁₂ -alkyl, or is C₁ -C₁₂ -acyl, or R₁ is a5-membered to 13-membered heterocyclic radical containing at least onenitrogen stom being linked to the

    --COCOOR.sub.2 radical,

said heterocyclic radical being selected from the group consisting ofpyrrolidinyl, piperidino, morpholino, 2,6-dimethylmorpholino,4-methylpiperazin-1-yl, 3,3,5,5-tetramethylpiperazin-1-yl,hexahydroazepin-1-yl and a radical of the formula ##STR82## with q=3-11;or if m=2, R₁ is a group ##STR83## in which R₆, R₈, R₉ and R₁₀ areidentical or different and are hydrogen, C₁ -C₁₈ -alkyl, C₅ -C₁₈-cycloalkyl unsubstituted or substituted by C₁ -C₁₂ -alkyl, C₃ -C₁₈-alkenyl, C₆ -C₁₈ -aryl unsubstituted or substituted by C₁ -C₁₂ -alkoxy,by C₁ -C₁₂ -alkyl and/or by --OH, C₇ -C₁₈ -aralkyl unsubstituted orsubstituted by C₁ -C₁₂ -alkyl and/or by --OH or are a group of theformula (II) and R₇ is C₂ -C₁₈ -alkylene, C₆ -C₁₈ -cycloalkylene, C₆-C₁₈ -arylene, C₇ -C₁₈ -aralkylene or a group --R₁₁ --X--(R₁₂ --X)_(n)--R₁₁ --, where R₁₁ and R₁₂ are identical or different and are C₂ -C₆-alkylene and X is --O-- or ##STR84## R₁₃ is hydrogen, C₁ -C₁₂ -alkyl,C₅ -C₁₂ -cycloalkyl unsubstituted or substituted by C₁ -C₁₂ -alkyl, oris a group of the formula (II) and n is zero, 1 or 2, or R₁ is a5-membered to 7-membered divalent heterocyclic group containing 2nitrogen atoms being linked to the

    --COCOOR.sub.2 radicals,

or if m=3, R₁ is a group ##STR85## in which R₁₄ and R₁₇ are identical ordifferent and are hydrogen, C₁ -C₁₈ -alkyl, C₅ -C₁₂ -cycloalkylunsubstituted or substituted by C₁ -C₁₂ -alkyl, C₇ -C₁₈ -aralkylunsubstituted or substituted by C₁ -C₁₂ -alkyl and/or by --OH or are agroup of the formula (II) and R₁₅ and R₁₆ are identical or different andare C₂ -C₆ -alkylene, or R₁ is a hexahydro-1,3,5-triazine-1,3,5-triylgroup, or if m=4, R₁ is a group ##STR86## in which R₁₈ and R₂₂ areidentical or different and are as defined for R₁₄ and R₁₇, while R₁₉,R₂₀ and R₂₁ are identical or different and are C₂ -C₆ -alkylene, or R₁is a group ##STR87## in which R₂₃, R₂₄, R₂₅ and R₂₆ are identical ordifferent and are C₂ -C₆ -alkylene; R₂ is C₁ -C₁₈ -alkyl, C₅ -C₁₈-cycloalkyl unsubstituted or substituted by C₁ -C₁₂ -alkyl, C₃ -C₁₈-alkenyl, C₆ -C₁₈ -aryl unsubstituted or substituted by C₁ -C₁₂ -alkoxy,by C₁ -C₁₂ -alkyl and/or by --OH, C₇ -C₁₈ -aralkyl unsubstituted orsubstituted by C₁ -C₁₂ -alkyl and/or by --OH, or is a group of theformula (II) or, if m is 1 and R₁ is a group ##STR88## R₂ additionallyis a group of the formula (III) ##STR89## wherein R₃ and R₅ are asdefined above and R₂₇ is C₂ -C₁₂ -alkylene, C₆ -C₁₈ -cycloalkylene orone of the following groups ##STR90## in which R₂₈ is hydrogen or C₁ -C₄-alkyl, R₂₉ is hydrogen, C₁ -C₄ -alkyl or a group ##STR91## R₃ and R₅are as defined in this claim and p is an integer from 1 to 4, at leastone group of the formula (II) being present in R₁ or R₂.
 2. Thecomposition according to claim 1, in which, if m is 1, R₁ is a group##STR92## in which R₃ and R₄ are identical or different and arehydrogen, C₁ -C₁₂ -alkyl, C₆ -C₁₂ -cycloalkyl, allyl, phenyl, benzyl ora group of the formula (II) in which R₅ is hydrogen, methyl, allyl,benzyl or acetyl, or R₁ is a heterocyclic radical selected from thegroup consisting of piperidino, morpholino and hexahydroazepin-1-yl; orif m is 2, R₁ is a group ##STR93## in which R₆ and R₈ are identical ordifferent and are hydrogen, C₁ -C₁₂ -alkyl, C₆ -C₉ -cycloalkyl or agroup of the formula (II) and R₇ is C₂ -C₁₂ -alkylene or a group --R₁₁--X--(R₁₂ --X)_(n) --R₁₁ -- in which R₁₁ and R₁₂ are identical ordifferent and are C₂ -C₆ -alkylene, X is --O-- and n is zero, 1 or 2, orR₁ is piperazine-1,4-diyl or 5,5,7-trimethylhomopiperazine-1,4-diyl; orif m is 3, R₁ is a group ##STR94## in which R₁₄ and R₁₇ are identical ordifferent and are hydrogen, C₁ -C₈ -alkyl, C₆ -C₉ -cycloalkyl or a groupof the formula (II) and R₁₅ and R₁₆ are identical or different and areC₂ -C₆ -alkylene, or R₁ is a hexahydro-1,3,5-triazine-1,3,5-triyl group;or if m is 4, R₁ is a group ##STR95## in which R₁₈ and R₂₂ are identicalor different and are hydrogen, C₁ -C₈ -alkyl, C₆ -C₉ -cycloalkyl or agroup of the formula (II) and R₁₉, R₂₀ and R₂₁ are identical ordifferent and are C₂ -C₆ -alkylene, or R₁ is a group ##STR96## R₂ is C₁-C₁₂ -alkyl, C₆ -C₉ -cycloalkyl, allyl, phenyl, benzyl or a group of theformula (II) or, if m is 1 and R₁ is a group ##STR97## with R₃ and R₅being as defined in this claim, R₂ additionally is a group of theformula (III) in which R₂₇ is C₂ -C₆ -alkylene, C₆ -C₁₂ -cycloalkyleneor one of the groups R₂₇ ', R₂₇ " and R₂₇ '" being as defined in claim1, wherein R₂₈ is hydrogen or methyl, R₂₉ is methyl, ethyl or a group##STR98## R₃ and R₅ are as defined in this claim and p is 1, with theproviso that at least one group of the formula (II) is present in R₁ orR₂.
 3. The composition according to claim 1, in which m is 1 or 2 and,if m is 1, R₁ is a group ##STR99## in which R₃ is hydrogen, C₁ -C₈-alkyl, cyclohexyl, 2,2,6,6-tetramethylpiperidin-4-yl or1,2,2,6,6-pentamethylpiperidin-4-yl and R₄ is2,2,6,6-tetramethylpiperidin-4-yl or1,2,2,6,6-pentamethylpiperidin-4-yl, or if m is 2, R₁ is a group##STR100## in which R₆ and R₈ are 2,2,6,6-tetramethylpiperidin-4-yl or1,2,2,6,6-pentamethylpiperidin-4-yl and R₇ is C₂ -C₆ -alkylene, or R₁ ispiperazine-1,4-diyl or 5,5,7-trimethylhomopiperazine-1,4-diyl, R₂ is2,2,6,6-tetramethylpiperidin-4-yl or1,2,2,6,6-pentamethylpiperidin-4-yl, or if m is 1 and R₁ is a group##STR101## R₂ additionally is one of the groups ##STR102## in which R₃is as defined in this claim and R₅ is hydrogen or methyl.
 4. Thecomposition of claim 1 containing compounds of the formula ##STR103## 5.The composition according to claim 1, in which m is
 1. 6. Thecomposition according to claim 1, in which m is
 2. 7. The compositionaccording to claim 1, wherein the organic material is a syntheticpolymer.
 8. The composition according to claim 7, wherein the syntheticpolymer is polyethylene or polypropylene.
 9. A method for stabilisingorganic material against oxidative, thermal and cationic degradationwhich comprises incorporating in said organic material on effectivestabilising amount of a compound according to claim 1.